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CASE REPORT article

Front. Med.

Sec. Obstetrics and Gynecology

Volume 12 - 2025 | doi: 10.3389/fmed.2025.1598144

When neuroglial tissue wanders: a unique case of subpleural heterotopia in a triploid foetus and review of the literature

Provisionally accepted
  • 1University Hospital Ostrava, Ostrava, Czechia
  • 2University Hospital in Motol, Prague, Prague, Czechia
  • 3University of Ostrava, Ostrava, Czechia

The final, formatted version of the article will be published soon.

Heterotopic occurrence of neuroglial tissue is an exceedingly rare phenomenon with unclear pathogenesis, often presenting as lesions outside the central nervous system (CNS). We report a unique case of heterotopic neuroglial tissue identified in the thoracic cavity of a foetus aborted at 14 weeks due to a suspected Dandy-Walker malformation. The foetus exhibited neuroglial tissue growth subpleurally, alongside a suspected Dandy-Walker malformation and ventricular septal defect. While theories such as vascular embolization, aspiration, and aberrant migration attempt to explain such occurrences, the exact aetiology remains elusive. Our case suggests a potential association between triploidy and neuroglial heterotopia, supporting the aberrant migration and differentiation theory.

Keywords: Brain heterotopia, Neural tube defect, Neuroglial heterotopia, Dandy-Walker malformation, Triploidy

Received: 22 Mar 2025; Accepted: 09 Sep 2025.

Copyright: © 2025 Procházka, Skopelidou, Delongová, Hurník, Špaček, Matura, Pavlíček, Gřegořová, Vaculová and Škarda. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Patricie Delongová, patricie.delongova@fno.cz

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